NDC codes

FDA NDC Directory
Product NDC (as listed)70710-1900Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70710-1900Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
70710-1900-37071019000330 TABLET in 1 BOTTLE (70710-1900-3)Marketed from Nov 30, 2023
70710-1900-97071019000990 TABLET in 1 BOTTLE (70710-1900-9)Marketed from Nov 30, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Sitagliptin
Generic name (nonproprietary)
sitagliptin
Active ingredients
Sitagliptin — 50 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 211566
Marketing start
Listing expires
Other FDA classes
Dipeptidyl Peptidase 4 Inhibitors (Mechanism)
Identifiers
Product ID 70710-1900_c489d9fa-c7f0-473f-9f7b-77086e137e8fSPL ID c489d9fa-c7f0-473f-9f7b-77086e137e8fSPL set ID 6a970e80-b753-48fa-9fff-87e7a5044982RxCUI 665033, 665038, 665042UNII QFP0P1DV7ZUPC 0370710190095

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470710190003 followed by a unit qualifier and the quantity

Package 70710-1900-03. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Sitagliptin Tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Limitations of Use Sitagliptin Tablets is not recommended in patients with type 1 diabetes mellitus. Sitagliptin Tablets have not been studied in patients with a history of pancreatitis. It is unknown whether patients with a history of pancreatitis are at increased risk for the development of pancreatitis while using Sitagliptin Tablets. [see Warnings and Precautions (5.1) ]. Sitagliptin Tablets are a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. ( …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 211566

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 211566
ProductStrengthForm · routeLabelerProduct NDC
SitagliptinSitagliptin 25 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1899
SitagliptinSitagliptin 100 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1901
ZituviositagliptinSitagliptin 50 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1241
ZituviositagliptinSitagliptin 25 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1240
ZituviositagliptinSitagliptin 100 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1242
ZituviositagliptinSitagliptin 50 mg/1TabletOralZydus Lifesciences Limited70771-1771
ZituviositagliptinSitagliptin 25 mg/1TabletOralZydus Lifesciences Limited70771-1770
ZituviositagliptinSitagliptin 100 mg/1TabletOralZydus Lifesciences Limited70771-1772
SitagliptinSitagliptin 25 mg/1TabletOralZydus Lifesciences Limited70771-1790
SitagliptinSitagliptin 50 mg/1TabletOralZydus Lifesciences Limited70771-1791
SitagliptinSitagliptin 100 mg/1TabletOralZydus Lifesciences Limited70771-1792

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